A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250087



Internal ID21311948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43602609..43684220hg38UCSC Ensembl
Outerchr15:43602608..43692744hg38UCSC Ensembl
Innerchr15:43894807..43976418hg19UCSC Ensembl
Outerchr15:43894806..43984942hg19UCSC Ensembl
Innerchr15:41682099..41763710hg18UCSC Ensembl
Outerchr15:41682098..41772234hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3890137
hg1990137
hg1890137
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169433
Supporting Variants
SamplesSNI_14
Known GenesCATSPER2, RNU6-28P, STRC
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250087
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer